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Alnus hirsuta

Alnus hirsuta - Unknown
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Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644038b620e51090163095
Scientific name Alnus hirsuta
Authority (Spach) Rupr.
First published in Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 15: 376 (1857)

Description Top

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Synonyms Top

Scientific name Authority First published in
Alnus sibirica f. hirsutoides Koidz. Bot. Mag. (Tokyo) 27: 145 1913
Alnus tinctoria var. microphylla Nakai Bot. Mag. (Tokyo) 42: 17 (1928)
Alnus tinctoria var. velutina H.Hara Bot. Mag. (Tokyo) 48: 805. 1934
Alnus tinctoria f. hirsutoides (Koidz.) H.Hara Bot. Mag. (Tokyo) 48: 804 1934
Alnus tinctoria var. glabra Callier Repert. Spec. Nov. Regni Veg. 10: 233. 1911
Alnus sibirica var. tinctoria (Sarg.) Koidz. Bot. Mag. (Tokyo) 27: 145. 1913
Alnus sibirica f. obtusiloba Koidz. Bot. Mag. (Tokyo) 27: 145 1913
Alnus sibirica f. acutiloba Koidz. Bot. Mag. (Tokyo) 27: 145 1913
Alnus sibirica f. glabra (Callier) Koidz. Bot. Mag. (Tokyo) 27: 145 1913
Alnus tinctoria f. acutiloba (Koidz.) H.Hara Bot. Mag. (Tokyo) 48: 805 1934
Alnus hirsuta f. macrophylla Callier Repert. Spec. Nov. Regni Veg. 10: 233 1911
Alnus tinctoria var. obtusiloba Callier Repert. Spec. Nov. Regni Veg. 10: 233. 1911
Alnus tinctoria var. mandschurica Callier Repert. Spec. Nov. Regni Veg. 10: 233. 1911
Alnus hirsuta f. inokumae (Murai & Kusaka) H.Ohba Fl. Japan 2a: 29 (2006)
Alnus hirsuta f. sibirica (Spach) H.Ohba Fl. Japan 2a: 29 (2006)
Alnus hirsuta var. microphylla (Nakai) Tatew. Res. Bull. Coll. Exp. Forests Coll. Agric. Hokkaido Imp. Univ. 7: 189. 1932
Alnus hirsuta var. sibirica (Spach) C.K.Schneid. Pl. Wilson. 2: 498 1916
Alnus incana subsp. hirsuta (Spach) Á.Löve & D.Löve Bot. Not. 128: 505 (1975 publ. 1976)
Alnus incana var. hirsuta Spach Ann. Sci. Nat., Bot. II, 15: 207 1841
Alnus incana var. sibirica Spach Ann. Sci. Nat., Bot. , sér. 2, 15: 207 (1841)
Alnus incana var. tinctoria (Sarg.) H.J.P.Winkl. Pflanzenr. IV, 61: 123. 1904
Alnus inokumae Murai & Kusaka Bull. Gov. Forest Exp. Sta. 141: 158, 166 (1962)
Alnus sibirica (Spach) Turcz. ex Kom. Trudy Imp. S.-Peterburgsk. Bot. Sada 22: 57. 1903 (1903)
Alnus sibirica var. hirsuta (Spach) Koidz. Bot. Mag. (Tokyo) 27: 144 1913
Alnus sibirica var. oxyloba C.K.Schneid. Ill. Handb. Laubholzk. 2: 891. 1912
Alnus sibirica var. paucinervis C.K.Schneid. Ill. Handb. Laubholzk. 2: 891. 1912
Alnus tinctoria Sarg. Gard. & Forest 10: 472 (1897)
Alnus sibirica Fisch. ex Turcz. Bull. Soc. Imp. Naturalistes Moscou 11(1): 101. 1838 ; 27. (1854) I. 406
Alnus incana var. glauca (F.Michx.) Loudon Arbor. Frutic. Brit. 3: 1688. 1838

Common names Top

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Language Common/alternative name
English siberian alder
English manchurian alder
Azerbaijani yumşaqtüklü qızılağac
Icelandic hæruölur
Korean 물오리나무
Dutch olsza szorstka
Polish olsza szorstka
Russian Ольха шерстистая
Russian Ольха пушистая
Turkish mançurya kızılağacı
Chinese 旱冬瓜
Chinese 色赤杨
Chinese 辽东桤木

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000945674
Tropicos 3600204
KEW urn:lsid:ipni.org:names:77176842-1
The Plant List kew-6410
PaleoBotany 70089
Open Tree Of Life 639096
Observations.org 128041
NCBI Taxonomy 109061
IUCN Red List 194610
IPNI 294926-1
iNaturalist 437257
GBIF 2876105
EPPO ALUHI
EOL 1145867
Elurikkus 2675
USDA GRIN 2450

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Worldwide forest surveys reveal forty-three new species in Phytophthora major Clade 2 with fundamental implications for the evolution and biogeography of the genus and global plant biosecurity Jung T, Milenković I, Balci Y, Janoušek J, Kudláček T, Nagy ZÁ, Baharuddin B, Bakonyi J, Broders KD, Cacciola SO, Chang TT, Chi NM, Corcobado T, Cravador A, Đorđević B, Durán A, Ferreira M, Fu CH, Garcia L, Hieno A, Ho HH, Hong C, Junaid M, Kageyama K, Kuswinanti T, Maia C, Májek T, Masuya H, Magnano di San Lio G, Mendieta-Araica B, Nasri N, Oliveira LS, Pane A, Pérez-Sierra A, Rosmana A, Sanfuentes von Stowasser E, Scanu B, Singh R, Stanivuković Z, Tarigan M, Thu PQ, Tomić Z, Tomšovský M, Uematsu S, Webber JF, Zeng HC, Zheng FC, Brasier CM, Horta Jung M Stud Mycol 27-Feb-2024
PMCID:PMC11003442
doi:10.3114/sim.2024.107.04
PMID:38600961
Classification, biosynthesis, and biological functions of triterpene esters in plants Liu J, Yin X, Kou C, Thimmappa R, Hua X, Xue Z Plant Commun 13-Feb-2024
PMCID:PMC11009366
doi:10.1016/j.xplc.2024.100845
PMID:38356259
Chemical Epigenetic Regulation Secondary Metabolites Derived from Aspergillus sydowii DL1045 with Inhibitory Activities for Protein Tyrosine Phosphatases Shi X, Li X, He X, Zhang D, Quan C, Xiu Z, Dong Y Molecules 31-Jan-2024
PMCID:PMC10856041
doi:10.3390/molecules29030670
PMID:38338416
Fine-Root Distribution and Soil Physicochemical Property Variations in Four Contrasting Urban Land-Use Types in South Korea Tran LT, An JY, Carayugan MB, Hernandez JO, Rahman SA, Youn WB, Carvalho JI, Jo MS, Han SH, Nguyen HH, Park BB Plants (Basel) 07-Jan-2024
PMCID:PMC10821101
doi:10.3390/plants13020164
PMID:38256718
Distribution, Effect, and Control of Exotic Plants in Republic of Korea Lim BS, Seok JE, Lim CH, Kim GS, Shin HC, Lee CS Biology (Basel) 06-Jun-2023
PMCID:PMC10294914
doi:10.3390/biology12060826
PMID:37372111
Betula mcallisteri sp. nov. (sect. Acuminatae, Betulaceae), a new diploid species overlooked in the wild and in cultivation, and its relation to the widespread B. luminifera Zhang H, Ding J, Holstein N, Wang N Front Plant Sci 23-May-2023
PMCID:PMC10268003
doi:10.3389/fpls.2023.1113274
PMID:37324661
Diarylheptanoids/sorafenib as a potential anticancer combination against hepatocellular carcinoma: the p53/MMP9 axis of action Elmetwalli A, Diab T, Albalawi AN, El-Naggar SA, El‑Far AH, Ghedan AR, Alamri ES, Salama AF Naunyn Schmiedebergs Arch Pharmacol 05-May-2023
PMCID:PMC10497687
doi:10.1007/s00210-023-02470-0
PMID:37145126
Cluster Composition of Anemophilous Plant Pollen Entering the Atmosphere Golovko VV, Zueva GA, Kiseleva TI 15-Dec-2022
PMCID:PMC9753010
doi:10.1134/S1024856022060136
Environmental stress - what can we learn from chlorophyll a fluorescence analysis in woody plants? A review Swoczyna T, Kalaji HM, Bussotti F, Mojski J, Pollastrini M Front Plant Sci 14-Dec-2022
PMCID:PMC9795016
doi:10.3389/fpls.2022.1048582
PMID:36589121
Taxonomic Review of the Genus Caloptilia Hübner, 1825 (Lepidoptera: Gracillariidae) with Descriptions of Three New Species and Seven Newly Recorded Species from Korea Kim DS, Shin YM, Lee JY, Byun BK Insects 30-Nov-2022
PMCID:PMC9785696
doi:10.3390/insects13121107
PMID:36555017
Analysis of Components and Properties of Extractives from Alnus cremastogyne Pods from Different Provenances Chen G, Pan F, Gao Y, Li H, Qin X, Jiang Y, Qi J, Xie J, Jia S Molecules 12-Nov-2022
PMCID:PMC9699184
doi:10.3390/molecules27227802
PMID:36431903
Differences in functional trait responses to elevation among feeding guilds of Aculeata community Uemori K, Mita T, Hishi T Ecol Evol 04-Aug-2022
PMCID:PMC9353017
doi:10.1002/ece3.9171
PMID:35949524
Physiological and Molecular Responses of Woody Plants Exposed to Future Atmospheric CO2 Levels under Abiotic Stresses Lobo AK, Catarino IC, Silva EA, Centeno DC, Domingues DS Plants (Basel) 20-Jul-2022
PMCID:PMC9322912
doi:10.3390/plants11141880
PMID:35890514
Commodity risk assessment of Acer palmatum plants grafted on Acer davidii from China Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 12-May-2022
PMCID:PMC9096882
doi:10.2903/j.efsa.2022.7298
PMID:35592020
Identification of Lagopus muta japonica food plant resources in the Northern Japan Alps using DNA metabarcoding Fujii T, Ueno K, Shirako T, Nakamura M, Minami M PLoS One 10-Mar-2022
PMCID:PMC8912148
doi:10.1371/journal.pone.0252632
PMID:35271584

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3aS,5aR,5bS,7aR,11aS,11bR,13aS,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 162943805 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(72)80041-4
> Phenylpropanoids and polyketides / Diarylheptanoids / Cyclic diarylheptanoids / Meta,para-diphenylether diarylheptanoids
(10R)-4,17-dimethoxy-2-oxatricyclo[13.2.2.13,7]icosa-1(17),3,5,7(20),15,18-hexaene-10,16-diol 10689752 Click to see COC1=C2C=C(CCC(CCCCC3=C(C(=C(O2)C=C3)OC)O)O)C=C1 358.40 unknown https://doi.org/10.1248/BPB.30.810
4,17-Dimethoxy-2-oxatricyclo[13.2.2.13,7]icosa-1(17),3,5,7(20),15,18-hexaene-10,16-diol 44567146 Click to see COC1=C2C=C(CCC(CCCCC3=C(C(=C(O2)C=C3)OC)O)O)C=C1 358.40 unknown https://doi.org/10.1248/BPB.30.810
Myricatomentogenin 10759713 Click to see COC1=C2C=CC(=C1O)CCCCC(=O)CCC3=CC(=C(C=C3)O)O2 342.40 unknown https://doi.org/10.1248/BPB.30.810
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2S,4S,6R)-2-[(1S)-1-hydroxy-2-(4-hydroxyphenyl)ethyl]-6-(4-hydroxy-3-methoxyphenyl)oxan-4-ol 46184734 Click to see COC1=C(C=CC(=C1)C2CC(CC(O2)C(CC3=CC=C(C=C3)O)O)O)O 360.40 unknown https://doi.org/10.1248/BPB.30.810
(4E)-1,7-Bis(3,4-dihydroxyphenyl)-4-hepten-3-one; 1,7-Bis-(3,4-dihydroxyphenyl)-4-hepten-3-one; Hirsutanone 66954880 Click to see C1=CC(=C(C=C1CCC=CC(=O)CCC2=CC(=C(C=C2)O)O)O)O 328.40 unknown https://doi.org/10.1248/BPB.30.810
1-(4-Hydroxyphenyl)-7-(4-hydroxy-3-methoxyphenyl)-4-hepten-3-one 78200757 Click to see COC1=C(C=CC(=C1)CCC=CC(=O)CCC2=CC=C(C=C2)O)O 326.40 unknown https://doi.org/10.1248/BPB.30.810
1,7-Bis(3,4-dihydroxyphenyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyheptan-3-one 14707657 Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)O)O)CC(=O)CCC3=CC(=C(C=C3)O)O)O)O)O 478.50 unknown https://doi.org/10.1016/0031-9422(92)80049-K
https://doi.org/10.1055/S-2000-8606
2-[1-Hydroxy-2-(4-hydroxyphenyl)ethyl]-6-(4-hydroxy-3-methoxyphenyl)oxan-4-ol 44567145 Click to see COC1=C(C=CC(=C1)C2CC(CC(O2)C(CC3=CC=C(C=C3)O)O)O)O 360.40 unknown https://doi.org/10.1248/BPB.30.810
2-[1,7-Bis(3,4-dihydroxyphenyl)heptan-3-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 75168353 Click to see C1=CC(=C(C=C1CCCCC(CCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 494.50 unknown https://doi.org/10.1055/S-2000-8606
2-[1,7-Bis(3,4-dihydroxyphenyl)heptan-3-yloxy]oxane-3,4,5-triol 74202880 Click to see C1C(C(C(C(O1)OC(CCCCC2=CC(=C(C=C2)O)O)CCC3=CC(=C(C=C3)O)O)O)O)O 464.50 unknown https://doi.org/10.1055/S-2000-8606
7-(4-Hydroxy-3-methoxy-phenyl)-1-(4-hydroxy-phenyl)-hept-4-en-3-one 637455 Click to see COC1=C(C=CC(=C1)CCC=CC(=O)CCC2=CC=C(C=C2)O)O 326.40 unknown https://doi.org/10.1248/BPB.30.810
Hirsutal 13347317 Click to see C1=CC(=C(C=C1CCC(CC(=O)CCC2=CC(=C(C=C2)O)O)O)O)O 346.40 unknown https://doi.org/10.1248/BPB.30.810
https://doi.org/10.1055/S-2000-8606
Hirsutanonol 9928190 Click to see C1=CC(=C(C=C1CCC(CC(=O)CCC2=CC(=C(C=C2)O)O)O)O)O 346.40 unknown https://doi.org/10.1248/BPB.23.517
https://doi.org/10.1007/BF02977009
https://doi.org/10.1007/BF02976466
https://doi.org/10.1248/BPB.30.810
https://doi.org/10.1055/S-2000-8606
Hirsutenone 637394 Click to see C1=CC(=C(C=C1CCC=CC(=O)CCC2=CC(=C(C=C2)O)O)O)O 328.40 unknown https://doi.org/10.1248/BPB.30.810
Oregonin 14707658 Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)O)O)CC(=O)CCC3=CC(=C(C=C3)O)O)O)O)O 478.50 unknown https://doi.org/10.1016/0031-9422(92)80195-K
https://doi.org/10.1248/BPB.23.517
https://doi.org/10.1055/S-2000-8606
https://doi.org/10.1016/0031-9422(92)80049-K
https://doi.org/10.1007/BF02976608
https://doi.org/10.1007/BF02976466
https://doi.org/10.1007/BF02977009
Rubranoside A 10097263 Click to see C1=CC(=C(C=C1CCCCC(CCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 494.50 unknown https://doi.org/10.1055/S-2000-8606
Rubranoside B 24011643 Click to see C1C(C(C(C(O1)OC(CCCCC2=CC(=C(C=C2)O)O)CCC3=CC(=C(C=C3)O)O)O)O)O 464.50 unknown https://doi.org/10.1055/S-2000-8606
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.3724/SP.J.1009.2012.00084
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
(2S,3S,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 44259219 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.3724/SP.J.1009.2012.00084
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.3724/SP.J.1009.2012.00084
> Phenylpropanoids and polyketides / Tannins
1,2,6-Trigalloyl-beta-D-glucopyranose 3357644 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 636.50 unknown https://doi.org/10.1016/0031-9422(92)80049-K
1,2,6-Trigalloylglucose 440308 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 636.50 unknown https://doi.org/10.1016/0031-9422(92)80049-K
1,4,6-tri-O-galloyl-beta-D-glucose 10077822 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 636.50 unknown https://doi.org/10.1016/0031-9422(92)80049-K
1,4,6-Trigalloyl-beta-D-glucopyranose 14284610 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 636.50 unknown https://doi.org/10.1016/0031-9422(92)80049-K
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate 5153915 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1016/0031-9422(92)80049-K
[4-[(3S)-7-(3,4-dihydroxyphenyl)-5-oxo-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyheptyl]-2-hydroxyphenyl] 2-[[(1R,2S,19R,20S,22R)-7,8,9,12,13,14,20,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]-3,4,5-trihydroxybenzoate 162974824 Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C7C(C(O6)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C15)O)O)O)O)O)O)O)O)O)CC(=O)CCC1=CC(=C(C=C1)O)O)O)O)O 1413.10 unknown https://doi.org/10.1016/0031-9422(92)80049-K
[4-[(3S)-7-(3,4-dihydroxyphenyl)-5-oxo-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyheptyl]-2-hydroxyphenyl] 2-[[(1R,2S,19R,22R)-7,8,9,12,13,14,20,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]-3,4,5-trihydroxybenzoate 16183111 Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C7C(C(O6)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C15)O)O)O)O)O)O)O)O)O)CC(=O)CCC1=CC(=C(C=C1)O)O)O)O)O 1413.10 unknown https://doi.org/10.1016/0031-9422(92)80195-K
[4-[7-(3,4-Dihydroxyphenyl)-5-oxo-3-(3,4,5-trihydroxyoxan-2-yl)oxyheptyl]-2-hydroxyphenyl] 2-[(7,8,9,12,13,14,20,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl)oxy]-3,4,5-trihydroxybenzoate 162974822 Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C7C(C(O6)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C15)O)O)O)O)O)O)O)O)O)CC(=O)CCC1=CC(=C(C=C1)O)O)O)O)O 1413.10 unknown https://doi.org/10.1016/0031-9422(92)80049-K
[6-(2,3-Dihydroxy-5-methoxycarbonylphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 14428078 Click to see COC(=O)C1=CC(=C(C(=C1)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)O 498.40 unknown https://doi.org/10.1016/0031-9422(92)80049-K
1-Desgalloyleugeniin 9918701 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1016/0031-9422(92)80049-K
2-[[(1R,2S,19R,20S,22R)-7,8,9,12,13,14,20,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]-3,4,5-trihydroxybenzoic acid 10033841 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)O)O)O)O)O)O)O)O)O 952.60 unknown https://doi.org/10.1016/0031-9422(92)80049-K
3-[(6-O-Galloyl-beta-D-glucopyranosyl)oxy]-4,5-dihydroxybenzoic acid methyl ester 10097402 Click to see COC(=O)C1=CC(=C(C(=C1)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)O 498.40 unknown https://doi.org/10.1016/0031-9422(92)80049-K
7,8,9,12,13,14,20,28,29,30,33,34,35-Tridecahydroxy-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaene-4,17,25,38-tetrone 492391 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/0031-9422(92)80049-K
alpha-Pedunculagin 13834142 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/0031-9422(92)80049-K
CID 14777390 14777390 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)O)O)O)O)O)O)O)O)O 952.60 unknown https://doi.org/10.1016/0031-9422(92)80195-K
CID 16174836 16174836 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C7C(C(O6)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O7)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1873.30 unknown https://doi.org/10.1016/0031-9422(92)80049-K
CID 16174839 16174839 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)OC9C(C(C1C(O9)COC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O 1721.20 unknown https://doi.org/10.1016/0031-9422(92)80049-K
Degalloylrugosin F 16174838 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)OC9C(C(C1C(O9)COC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O 1721.20 unknown https://doi.org/10.1016/0031-9422(92)80195-K
https://doi.org/10.1016/0031-9422(92)80049-K
Pedunculagin 442688 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/0031-9422(92)80195-K
Praecoxin A 14777391 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)O)O)O)O)O)O)O)O)O 952.60 unknown https://doi.org/10.1016/0031-9422(92)80049-K
Rugosin F 16174837 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C7C(C(O6)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O7)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1873.30 unknown https://doi.org/10.1016/0031-9422(92)80049-K
https://doi.org/10.1016/0031-9422(92)80195-K

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